GUDIDData
eudamed_udi Primary ID: 00860005590230

Breezing Med (UDI 00860005590230)

Manufactured by TF Health Corp

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Breezing Med - Primary ID 00860005590230

Device Regulatory Overview

The Breezing Med (Model/Catalog Number: 602intern) is a medical device manufactured by TF Health Corp. This product is indexed under FDA Product Code / Category Classification Z1203020404 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
602intern
Product Code / EMDN
Z1203020404
Device Name
Breezing Med
Database Sync Date
2026-08-09 18:00:55

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Breezing Med?

The registered manufacturer of record for Breezing Med is TF Health Corp.

What is the Primary UDI-DI identifier for Breezing Med?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00860005590230.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020404.

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